Novel Generation ofo-Quinone Methides on the Basis of Lewis Acid Catalyzed 1,4-Dethiolation ofo-(1-(Alkylthio)alkyl)phenols
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/19/1/19_1_55/_pdf
Reference23 articles.
1. Heterodiene syntheses with .alpha.,.beta.-unsaturated carbonyl compounds
2. Photolysis of 2-keto-2,3-dihydrobenzofurans, o-hydroxystyrenes and 1-(o-hydroxyphenyl)-1,5-hexadienes
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1. Development of Regioselective Inverse-Electron-Demand [4+2] Cycloaddition with Electron-Rich Arylalkynes for Access to Multi-Substituted Condensed Oxapolycyclic Compounds;Journal of Synthetic Organic Chemistry, Japan;2018-12-01
2. Catalytic Asymmetric Intramolecular [4+2] Cycloaddition of In Situ Generated ortho -Quinone Methides;Angewandte Chemie International Edition;2017-02-17
3. Katalytisch-asymmetrische intramolekulare [4+2]-Cycloaddition von in situ generierten ortho -Chinonmethiden;Angewandte Chemie;2017-02-17
4. RECENT ADVANCES IN CATALYTIC ASYMMETRIC CYCLOADDITION REACTIONS OF ortho-QUINONE METHIDES FOR SYNTHESIS OF O-HETEROCYCLES;TARG HETEROCYCL SYST;2017
5. Ortho-Quinone Methides as Reactive Intermediates in Asymmetric Brønsted Acid Catalyzed Cycloadditions with Unactivated Alkenes by Exclusive Activation of the Electrophile;Angewandte Chemie International Edition;2015-03-17
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